FDA 510(k) Applications Submitted by HDI, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K222741 09/09/2022 DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular, Fast) HDI, Inc.
K213339 10/07/2021 DENU Composite Resin, DENU Flow Resin HDI, Inc.


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